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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148187copy number variation1nstd102humanPathogenic GRCh38 chr1: 224,304,638-224,434,886 , GRCh37.p13 chr1: 224,492,340-224,622,588 NVL, CNIH4, 4 more genes
    nsv7147341insertion1nstd232human GRCh37.p13 chr1: 224,585,932-224,585,932 , GRCh38.p12 chr1: 224,398,230-224,398,230 WDR26, MIR4742
    nsv7146589copy number variation1nstd232human GRCh37.p13 chr1: 224,619,282-224,619,381 , GRCh38.p12 chr1: 224,431,580-224,431,679 WDR26
    nsv7138019insertion1nstd232human GRCh37.p13 chr1: 224,592,273-224,592,273 , GRCh38.p12 chr1: 224,404,571-224,404,571 WDR26
    nsv7099264copy number variation1nstd231human GRCh38.p12 chr1: 222,151,895-226,849,338 , GRCh37 chr1: 222,325,237-227,037,039 PARP1, CAPN2, 99 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv6675709copy number variation1nstd229human GRCh38 chr1: 224,161,301-224,385,400 , GRCh37.p13 chr1: 224,349,003-224,573,102 LOC101927164, FBXO28, 8 more genes
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636736copy number variation1nstd102humanUncertain significance GRCh37 chr1: 221,325,488-225,804,228 , GRCh38.p12 chr1: 221,152,146-225,616,526 BROX, LINC02765, 77 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6552060inversion1nstd223human GRCh38 chr1: 224,403,113-224,403,655 , GRCh37.p13 chr1: 224,590,815-224,591,357 WDR26
    nsv6550492inversion1nstd223human GRCh38 chr1: 224,409,997-224,410,992 , GRCh37.p13 chr1: 224,597,699-224,598,694 WDR26
    nsv6550176inversion1nstd223human GRCh38 chr1: 224,383,834-224,384,673 , GRCh37.p13 chr1: 224,571,536-224,572,375 WDR26
    nsv6547038inversion1nstd223human GRCh38 chr1: 224,407,007-224,407,808 , GRCh37.p13 chr1: 224,594,709-224,595,510 WDR26
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6327546copy number variation1nstd223human GRCh38 chr1: 224,389,115-224,389,670 , GRCh37.p13 chr1: 224,576,817-224,577,372 WDR26
    nsv6324615copy number variation1nstd223human GRCh38 chr1: 221,964,560-227,275,239 , GRCh37.p13 chr1: 222,137,902-227,462,940 LEFTY2, HHIPL2, 109 more genes
    nsv6315349copy number variation1nstd102humanPathogenic GRCh37 chr1: 224,432,682-225,142,704 , GRCh38.p12 chr1: 224,244,980-224,955,002 DNAJB6P6, CNIH3, 13 more genes
    nsv6313779copy number variation1nstd102humanPathogenic GRCh37 chr1: 221,303,919-227,461,343 , GRCh38.p12 chr1: 221,130,577-227,273,642 ENAH, HHIPL2, 119 more genes
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